Research Topic · Peer-Reviewed

Autosomal Dominant Diseases

Autosomal dominant Diseases are genetic disorders caused by a single mutated allele (a variant form of a gene). These mutations can be inherited from one parent or can occur spontaneously in the offspring. They can affect multiple organ systems throughout the body and are typically seen in adults. Examples of autoso…

Curated from this journal's research 📚 1 peer-reviewed article cited 🔖 ISSN 2997-1977 🗓 Reviewed July 2026

Overview

Autosomal dominant Diseases are genetic disorders caused by a single mutated allele (a variant form of a gene). These mutations can be inherited from one parent or can occur spontaneously in the offspring. They can affect multiple organ systems throughout the body and are typically seen in adults. Examples of autosomal dominant Diseases include Huntington’s Disease, Marfan Syndrome, and Neurofibromatosis. These Diseases can cause serious health issues, including physical deformities, organ dysfunction, and cognitive impairment. Early diagnosis and treatment is essential to managing and reducing the severity of symptoms. With advancements in medical technology, there are many treatment options available for those who suffer from autosomal dominant Diseases.

Research published in this journal

1 peer-reviewed article, ranked by relevance. Each links to its DOI.

Editorial oversight

Curated from peer-reviewed research published in Diseases (ISSN 2997-1977).

Journal editorial board
Madalena Barroso · Germany VASSILIKI PITIRIGA · Greece Andrzej Prystupa · Poland

This page summarises published research for orientation; it is not medical or professional advice.